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FDA 510(k)

MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7

K-Number: K982821 · 1998-11-05

ApplicantMultimedia Medical Systems, Inc.
Decision Date1998-11-05
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7 is the device name listed in this FDA 510(k) record. The listed applicant is Multimedia Medical Systems, Inc.. It received FDA 510(k) clearance on 1998-11-05 under 510(k) number K982821. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7?

MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7 is a medical device that received FDA 510(k) clearance on 1998-11-05. The listed applicant is Multimedia Medical Systems, Inc.. The 510(k) number is K982821.

When did MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7 receive FDA 510(k) clearance?

MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7 received FDA 510(k) clearance on 1998-11-05, under 510(k) number K982821.

Who is the listed applicant for MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7?

The FDA 510(k) record lists Multimedia Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7?

The FDA product code for MMS THERPACPLUS B3DTUI MODEL NUMBER 6.7 is MUJ.

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Related Devices (Code: MUJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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